Figure 5
Figure 5. NKG2A educates reconstituting post-HCT NK cells for degranulation but not for cytokine production. CD56+CD3−–gated NK cells from donor and post-HCT recipient pairs receiving T-cell replete transplants were further gated as KIR−NKG2A− (light gray bars), KIR−NKG2A+ (white bars), KIR+NKG2A+ (dark gray bars), or KIR+NKG2A− (black bars) based on staining with a cocktail of KIR antibodies and NKG2A. CD107a expression and IFNγ production were measured on all 4 subsets after incubation with K562 cells for 4 hours. IFNγ also was measured after overnight stimulation with IL-12 and IL-18. Bars represent the mean ± SEM. Pairwise comparisons were based on a linear mixed model. Statistical significance is indicated as *P < .05, **P < .01, and ***P < .0001. ns = not significant. NE = not evaluable.

NKG2A educates reconstituting post-HCT NK cells for degranulation but not for cytokine production. CD56+CD3–gated NK cells from donor and post-HCT recipient pairs receiving T-cell replete transplants were further gated as KIRNKG2A (light gray bars), KIRNKG2A+ (white bars), KIR+NKG2A+ (dark gray bars), or KIR+NKG2A (black bars) based on staining with a cocktail of KIR antibodies and NKG2A. CD107a expression and IFNγ production were measured on all 4 subsets after incubation with K562 cells for 4 hours. IFNγ also was measured after overnight stimulation with IL-12 and IL-18. Bars represent the mean ± SEM. Pairwise comparisons were based on a linear mixed model. Statistical significance is indicated as *P < .05, **P < .01, and ***P < .0001. ns = not significant. NE = not evaluable.

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